Solid-phase molecularly imprinted pre-concentration and spectrophotometric determination of isoxicam in pharmaceuticals and human serum

被引:24
|
作者
Rezaei, B. [1 ]
Mallakpour, S. [1 ]
Majidi, N. [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 8415683111, Iran
关键词
Molecularly imprinted polymer; Isoxicam; Spectrophotometry; Pharmaceutical and biological samples; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; LIQUID-CHROMATOGRAPHIC ANALYSIS; HUMAN-PLASMA; ALZHEIMERS-DISEASE; COLORECTAL-CANCER; EXTRACTION; PREVENTION; TENOXICAM; PIROXICAM; POLYMERS;
D O I
10.1016/j.talanta.2008.11.042
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A selective molecularly imprinted polymer (MIP) has been synthesized for isoxicam pre-concentration, followed by its spectrophotometric determination based on hydrogen bonding interactions between examined drug and alizarin yellow GG. This method is able to evaluate isoxicam in range of 1.0 x 10(-3) to 20.0 mu g mL(-1), with a limit of determination of 1.0 ng mL(-1). The retention capacity and pre-concentration factor of prepared sorbent are 18.5 mg g(-1) and 200, respectively; and the prepared MIPs can be reused at least for five times. The MIP capability for isoxicam selection and extraction from the solution is higher than non-imprinted polymer(NIP). Under optimum conditions, this procedure can be successfully applied to assay trace amounts of isoxicam in pharmaceutical and biological samples. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:418 / 423
页数:6
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